Survival, re-expansion, and pregnancy outcome following vitrification of dromedary camel cloned blastocysts: A possible role of vitrification in improving clone pregnancy rate by weeding out poor competent embryos
| Autor: | F. Moulavi, S.M. Hosseini, B. Asadi-Moghaddam, Sofia Soto-Rodriguez, Masashige Kuwayama |
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| Rok vydání: | 2019 |
| Předmět: |
Blastomeres
animal structures Camelus Cryoprotectant Pregnancy Rate Cloning Organism Biology General Biochemistry Genetics and Molecular Biology Cryopreservation Andrology 03 medical and health sciences 0302 clinical medicine Cryoprotective Agents In vivo Pregnancy Freezing medicine Animals Humans Vitrification 030219 obstetrics & reproductive medicine 0402 animal and dairy science Pregnancy Outcome Embryo 04 agricultural and veterinary sciences General Medicine Blastomere medicine.disease Embryo Transfer Embryo Mammalian 040201 dairy & animal science Pregnancy rate Blastocyst embryonic structures Female General Agricultural and Biological Sciences |
| Zdroj: | Cryobiology. 90 |
| ISSN: | 1090-2392 |
| Popis: | There is a clinical demand for efficient cryopreservation of cloned camel embryos with considerable logistic and economic advantage. Vitrification of in vivo derived embryos has been reported in camels, but there is no study on vitrification of cloned embryos. Moreover, whether characteristic differences between cloned and in vivo derived embryos imply different vitrification requirement is unresolved. Here, we compared survival, re-expansion and pregnancy rates of cloned embryos vitrified using two commercial vitrification kits (Cryotec and Kitazato), developed basically for human embryos, and a vitrification protocol developed for in vivo camel embryos (CVP). Cloned embryos responded dynamically to vitrification-warming steps in commercial kits, with a flat shrinkage in the final vitrification solution and a quick re-expansion to the original volume immediately after transferring to the isotonic warming solution. Contrarily, full shrinkage was not observed in CVP method, and majority of embryos were still collapsed post-warming. The immediate re-expansion was highly associated and predictive of higher survival and total cell number, and also better redox state of embryos vitrified by Cryotec and Kitazato kits compared to CVP method. Importantly, while 30% blastomere loss, verified by differential dye exclusion test, was tolerated in vitrified embryos, >50% blastomeres loss in non-expanded blastocysts implied the minimal essential cell survival rate for blastocoelic cavity re-expansion in vitrified cloned camel blastocysts, irrespective of vitrification method. A protocol-based exposure of embryos to cryoprotectants indicated that cryoprotectant toxicity, per se, may not be involved in lower cryosurvival of embryos in CVP vs. Cryotec and Kitazato. The initial pregnancy rates were numerically higher in Cryotec and Kitazato frozen transfers compared to fresh transfer (56.3, 60 and 33.3%, respectively), and importantly, a higher percentage of established pregnancies in vitrified groups passed the critical 3 months period of early embryonic loss compared to sibling fresh clone pregnancies (50, 40, and 10%, respectively). Results confirmed the suitability of Cryotec and Kitazato kits for vitrification of cloned camel embryos and that vitrification may improve pregnancy outcome by weeding out poor competent embryos. |
| Databáze: | OpenAIRE |
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